Variant report

Variant	esv1831862
Chromosome Location	chr18:14434450-14460476
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr18:14448468-14448755	GM12878	blood:	n/a	n/a
2	CEBPB	chr18:14458091-14458453	HepG2	liver:	n/a	n/a
3	CTCF	chr18:14458030-14458146	Kidney_OC	kidney:	n/a	chr18:14458126-14458139
4	CTCF	chr18:14460002-14460024	NHEK	skin:	n/a	n/a
5	CTCF	chr18:14458800-14458950	HCT-116	colon:	n/a	chr18:14458834-14458847
6	CTCF	chr18:14458680-14458830	AoAF	blood vessel:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
7	CTCF	chr18:14458680-14458830	HepG2	liver:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
8	CTCF	chr18:14450378-14450406	Lung_OC	lung:	n/a	n/a
9	CTCF	chr18:14457985-14458184	MCF-7	breast:	n/a	chr18:14458126-14458139
10	CTCF	chr18:14458624-14458839	HepG2	liver:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
11	CTCF	chr18:14459880-14460030	K562	blood:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
12	CTCF	chr18:14450231-14450429	Pancreas_OC	pancreas:	n/a	chr18:14450334-14450347
13	CTCF	chr18:14458638-14458861	GM20000	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
14	CTCF	chr18:14458656-14458847	GM19240	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
15	CTCF	chr18:14447405-14447461	Lung_OC	lung:	n/a	n/a
16	CTCF	chr18:14448220-14448370	HEK293	kidney:	n/a	chr18:14448296-14448309
17	CTCF	chr18:14459880-14460030	SK-N-SH_RA	brain:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
18	CTCF	chr18:14458626-14458889	LNCaP	prostate:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
19	CTCF	chr18:14448454-14448512	LNCaP	prostate:	n/a	n/a
20	CTCF	chr18:14458540-14458690	GM12870	blood:	n/a	n/a
21	CTCF	chr18:14459971-14460026	MCF-7	breast:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
22	CTCF	chr18:14458031-14458128	MCF-7	breast:	n/a	n/a
23	CTCF	chr18:14458680-14458830	GM12874	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
24	CTCF	chr18:14457986-14458160	MCF-7	breast:	n/a	chr18:14458126-14458139
25	CTCF	chr18:14458160-14458310	GM06990	blood:	n/a	n/a
26	CTCF	chr18:14458660-14458810	GM12878	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
27	CTCF	chr18:14458645-14458867	NHEK	skin:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
28	CTCF	chr18:14448295-14448342	MCF-7	breast:	n/a	chr18:14448296-14448309
29	CTCF	chr18:14458680-14458830	HUVEC	blood vessel:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
30	CTCF	chr18:14458654-14458848	GM12892	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
31	CTCF	chr18:14458080-14458230	GM12873	blood:	n/a	chr18:14458126-14458139
32	CTCF	chr18:14458600-14458750	GM12871	blood:	n/a	chr18:14458743-14458750
33	CTCF	chr18:14458920-14459070	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr18:14458616-14458889	Pancreas_OC	pancreas:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
35	CTCF	chr18:14458614-14458868	Lung_OC	lung:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
36	CTCF	chr18:14458680-14458830	HPF	lung:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
37	CTCF	chr18:14458600-14458750	GM12865	blood:	n/a	chr18:14458743-14458750
38	CTCF	chr18:14458680-14458830	HA-sp	spinal cord:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
39	CTCF	chr18:14458140-14458290	HRE	kidney:	n/a	n/a
40	CTCF	chr18:14458652-14458818	Gliobla	brain:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
41	CTCF	chr18:14458700-14458850	AG04449	skin:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458834-14458847 chr18:14458743-14458750
42	CTCF	chr18:14458680-14458830	AG10803	skin:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
43	CTCF	chr18:14458001-14458168	LNCaP	prostate:	n/a	chr18:14458126-14458139
44	CTCF	chr18:14458600-14458750	GM12872	blood:	n/a	chr18:14458743-14458750
45	CTCF	chr18:14459906-14460086	A549	lung:	n/a	chr18:14459995-14460013 chr18:14459998-14460011
46	CTCF	chr18:14458680-14458830	AG09309	skin:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
47	CTCF	chr18:14458600-14458750	HCM	heart:	n/a	chr18:14458743-14458750
48	CTCF	chr18:14458600-14458750	HMEC	breast:	n/a	chr18:14458743-14458750
49	CTCF	chr18:14458549-14458843	K562	blood:	n/a	chr18:14458737-14458753 chr18:14458736-14458754 chr18:14458743-14458750
50	CTCF	chr18:14459734-14460167	SK-N-SH	brain:	n/a	chr18:14459995-14460013 chr18:14459998-14460011

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:14450199-14450249	NHBE	bronchial:	n/a
2	chr18:14451035-14451085	NH-A	brain:	n/a
3	chr18:14450199-14450249	SAEC	small airway:	n/a
4	chr18:14450194-14450244	CMK	blood:	n/a
5	chr18:14450194-14450244	NHBE	bronchial:	n/a
6	chr18:14458927-14458977	HUVEC	blood vessel:	n/a
7	chr18:14457820-14457870	A549	lung:	n/a
8	chr18:14435120-14435170	BJ	skin:	n/a
9	chr18:14459174-14459224	PrEC	prostate:	n/a
10	chr18:14450799-14450849	Hela-S3	cervix:	n/a
11	chr18:14459174-14459224	AG04449	skin:	fetal
12	chr18:14459174-14459224	HEK293	kidney:	embryo
13	chr18:14450799-14450849	HEEpiC	esophagus:	n/a
14	chr18:14450199-14450249	SK-N-MC	brain:	n/a
15	chr18:14435120-14435170	NT2-D1	testis:	n/a
16	chr18:14455307-14455357	PFSK-1	brain:	n/a
17	chr18:14457820-14457870	GM12878	blood:	n/a
18	chr18:14450799-14450849	Caco-2	colon:	n/a
19	chr18:14458692-14458742	SAEC	small airway:	n/a
20	chr18:14458692-14458742	HUVEC	blood vessel:	n/a
21	chr18:14447545-14447595	HCPEpiC	choroid plexus:	n/a
22	chr18:14458692-14458742	AG04450	lung:	fetal
23	chr18:14459174-14459224	HMEC	breast:	n/a
24	chr18:14450199-14450249	HIPEpiC	eye:	n/a
25	chr18:14451035-14451085	HepG2	liver:	n/a
26	chr18:14459174-14459224	NB4	blood:	n/a
27	chr18:14459044-14459094	HIPEpiC	eye:	n/a
28	chr18:14459044-14459094	SAEC	small airway:	n/a
29	chr18:14455307-14455357	GM12892	blood:	n/a
30	chr18:14455307-14455357	AG10803	skin:	n/a
31	chr18:14458161-14458211	HRE	kidney:	n/a
32	chr18:14458692-14458742	CMK	blood:	n/a
33	chr18:14457820-14457870	HRPEpiC	eye:	n/a
34	chr18:14458692-14458742	AG09309	skin:	n/a
35	chr18:14458927-14458977	HIPEpiC	eye:	n/a
36	chr18:14457820-14457870	HEK293	kidney:	embryo
37	chr18:14450199-14450249	K562	blood:	n/a
38	chr18:14459044-14459094	K562	blood:	n/a
39	chr18:14435120-14435170	PrEC	prostate:	n/a
40	chr18:14455307-14455357	AG09309	skin:	n/a
41	chr18:14450799-14450849	AG10803	skin:	n/a
42	chr18:14459174-14459224	LNCaP	prostate:	n/a
43	chr18:14450199-14450249	SK-N-SH	brain:	n/a
44	chr18:14459174-14459224	HNPCEpiC	eye:	n/a
45	chr18:14450199-14450249	AG04450	lung:	fetal
46	chr18:14458692-14458742	HNPCEpiC	eye:	n/a
47	chr18:14455307-14455357	AoSMC	blood vessel:	n/a
48	chr18:14435120-14435170	HCPEpiC	choroid plexus:	n/a
49	chr18:14459174-14459224	HIPEpiC	eye:	n/a
50	chr18:14458692-14458742	HepG2	liver:	n/a

Variant related genes	Relation type
LONRF2P1	TF binding region
LONRF2P1	CpG island

Extended variants
information (count: 473 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8094801	chr18:14434450-14434451	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139862046	chr18:14434475-14434476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543475156	chr18:14434479-14434480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563463132	chr18:14434517-14434518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs10853249	chr18:14434521-14434522	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs552527627	chr18:14434527-14434528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34392140	chr18:14434531-14434532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566351083	chr18:14434545-14434546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532705892	chr18:14434572-14434573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528829028	chr18:14434585-14434586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201839878	chr18:14434617-14434618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62080604	chr18:14434619-14434620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs567238984	chr18:14434687-14434688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112441805	chr18:14434690-14434691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536276788	chr18:14434739-14434740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367585810	chr18:14434741-14434742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556275405	chr18:14434747-14434748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569804775	chr18:14434756-14434757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538818577	chr18:14434759-14434760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376041735	chr18:14434764-14434765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558518426	chr18:14434781-14434782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184685339	chr18:14434788-14434789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534574109	chr18:14434814-14434815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200527622	chr18:14434853-14434854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554457862	chr18:14434866-14434867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574463922	chr18:14434926-14434927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562984812	chr18:14434953-14434954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543440037	chr18:14434991-14434992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188155809	chr18:14435003-14435004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577304681	chr18:14435011-14435012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546373214	chr18:14435094-14435095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559641589	chr18:14435113-14435114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147956781	chr18:14435121-14435122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548872938	chr18:14435154-14435155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562397856	chr18:14435170-14435171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529700938	chr18:14435191-14435192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549845272	chr18:14435198-14435199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569764161	chr18:14435204-14435205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538308970	chr18:14435298-14435299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552260014	chr18:14435299-14435300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35928226	chr18:14435352-14435353	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs185719274	chr18:14435365-14435366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9965279	chr18:14435480-14435481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554421083	chr18:14435579-14435580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62080605	chr18:14435605-14435606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574424998	chr18:14435609-14435610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189684385	chr18:14435610-14435611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556980679	chr18:14435621-14435622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374564931	chr18:14435636-14435637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372804195	chr18:14435679-14435680	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14431600-14435000	Weak transcription	Osteobl	bone
2	chr18:14431600-14435200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr18:14435000-14435200	Enhancers	Osteobl	bone
4	chr18:14435200-14435600	Weak transcription	Osteobl	bone
5	chr18:14435200-14436200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr18:14435600-14436000	Enhancers	Osteobl	bone
7	chr18:14448800-14450400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr18:14449400-14449600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr18:14449400-14449600	Enhancers	Pancreas	Pancrea
10	chr18:14449400-14449800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
11	chr18:14449600-14451000	Active TSS	HSMM	muscle
12	chr18:14450000-14450200	Enhancers	Adipose Nuclei	Adipose
13	chr18:14450000-14450200	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr18:14450000-14450200	Flanking Active TSS	Stomach Smooth Muscle	stomach
15	chr18:14450000-14450600	Enhancers	Primary T cells fromperipheralblood	blood
16	chr18:14450000-14451000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr18:14450000-14451000	Active TSS	Brain Germinal Matrix	brain
18	chr18:14450000-14451000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr18:14450000-14451000	Active TSS	Colonic Mucosa	Colon
20	chr18:14450000-14451000	Active TSS	Colon Smooth Muscle	Colon
21	chr18:14450000-14451000	Active TSS	Fetal Brain Female	brain
22	chr18:14450000-14451200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr18:14450200-14450400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
24	chr18:14450200-14450400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr18:14450200-14450800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
26	chr18:14450200-14450800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr18:14450200-14451000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr18:14450200-14451000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr18:14450200-14451000	Active TSS	Breast Myoepithelial Primary Cells	Breast
30	chr18:14450200-14451000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr18:14450200-14451000	Active TSS	Muscle Satellite Cultured Cells	--
32	chr18:14450200-14451000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr18:14450200-14451000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr18:14450200-14451000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr18:14450200-14451000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr18:14450200-14451000	Active TSS	Adipose Nuclei	Adipose
37	chr18:14450200-14451000	Active TSS	Brain Angular Gyrus	brain
38	chr18:14450200-14451000	Active TSS	Brain Hippocampus Middle	brain
39	chr18:14450200-14451000	Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr18:14450200-14451000	Active TSS	Esophagus	oesophagus
41	chr18:14450200-14451000	Active TSS	Left Ventricle	heart
42	chr18:14450200-14451000	Active TSS	Pancreas	Pancrea
43	chr18:14450200-14451000	Active TSS	Right Ventricle	heart
44	chr18:14450200-14451000	Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr18:14450200-14451000	Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr18:14450200-14451000	Active TSS	Stomach Smooth Muscle	stomach
47	chr18:14450200-14451200	Active TSS	HMEC	breast
48	chr18:14450200-14453400	Active TSS	Osteobl	bone
49	chr18:14450400-14450800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
50	chr18:14450400-14451000	Active TSS	iPS-18 Cell Line	embryonic stem cell

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